Aims. This study aimed to determine the minimal detectable change (MDC), minimal clinically important difference (MCID), and substantial clinical benefit (SCB) under distribution- and anchor-based methods for the Mayo Elbow Performance Index (MEPI) and range of movement (ROM) after open elbow arthrolysis (OEA). We also assessed the proportion of patients who achieved MCID and SCB; and identified the factors associated with achieving MCID. Methods. A cohort of 265 patients treated by OEA were included. The MEPI and ROM were evaluated at baseline and at two-year follow-up. Distribution-based MDC was calculated with confidence intervals (CIs) reflecting 80% (MDC 80), 90% (MDC 90), and 95% (MDC 95) certainty, and MCID with changes from baseline to follow-up. Anchor-based MCID (anchored to somewhat satisfied) and SCB (very satisfied) were calculated using a five-level Likert satisfaction scale. Multivariate logistic regression of factors affecting MCID achievement was performed. Results. The MDC increased substantially based on selected CIs (MDC 80, MDC 90, and MDC 95), ranging from 5.0 to 7.6 points for the MEPI, and from 8.2° to 12.5° for ROM. The MCID of the MEPI were 8.3 points under distribution-based and 12.2 points under anchor-based methods; distribution- and anchor-based MCID of ROM were 14.1° and 25.0°. The SCB of the MEPI and ROM were 17.3 points and 43.4°, respectively. The proportion of the patients who attained anchor-based MCID for the MEPI and ROM were 74.0% and 94.7%, respectively; furthermore, 64.2% and 86.8% attained SCB. Non-dominant arm (p = 0.022), higher preoperative MEPI rating (p < 0.001), and postoperative visual analogue scale pain score (p < 0.001) were independent predictors of not achieving MCID for the MEPI, while atraumatic causes (p = 0.040) and higher preoperative ROM (p = 0.005) were independent risk factors for ROM. Conclusion. In patients undergoing OEA, the MCID for the increased MEPI is 12.2 points and 25° increased ROM. The SCB is 17.3 points and 43.3°, respectively. Future studies using the MEPI and ROM to assess OEA outcomes should report not only statistical significance but also clinical importance. Cite this article: Bone Joint J 2021;103-B(2):366–372

Aims. The aim of this study was to report the meaningful values of the EuroQol five-dimension three-level questionnaire (EQ-5D-3L) and EuroQol visual analogue scale (EQ-VAS) in patients undergoing primary knee arthroplasty (KA). Methods. This is a retrospective study of patients undergoing primary KA for osteoarthritis in a university teaching hospital (Royal Infirmary of Edinburgh) (1 January 2013 to 31 December 2019). Pre- and postoperative (one-year) data were prospectively collected for 3,181 patients (median age 69.9 years (interquartile range (IQR) 64.2 to 76.1); females, n = 1,745 (54.9%); median BMI 30.1 kg/m. 2. (IQR 26.6 to 34.2)). The reliability of the EQ-5D-3L was measured using Cronbach’s alpha. Responsiveness was determined by calculating the anchor-based minimal clinically important difference (MCID), the minimal important change (MIC) (cohort and individual), the patient-acceptable symptom state (PASS) predictive of satisfaction, and the minimal detectable change at 90% confidence intervals (MDC-90). Results. The EQ-5D-3L demonstrated good internal consistency with an overall Cronbach alpha of 0.75 (preoperative) and 0.88 (postoperative), respectively. The MCID for the Index score was 0.085 (95% confidence interval (CI) 0.042 to 0.127) and EQ-VAS was 6.41 (95% CI 3.497 to 9.323). The MIC. COHORT. was 0.289 for the EQ-5D and 5.27 for the EQ-VAS. However, the MIC. INDIVIDUAL. for both the EQ-5D-3L Index (0.105) and EQ-VAS (-1) demonstrated poor-to-acceptable reliability. The MDC-90 was 0.023 for the EQ-5D-3L Index and 1.0 for the EQ-VAS. The PASS for the postoperative EQ-5D-3L Index and EQ-VAS scores predictive of patient satisfaction were 0.708 and 77.0, respectively. Conclusion. The meaningful values of the EQ-5D-3L Index and EQ-VAS scores can be used to measure clinically relevant changes in health-related quality of life in patients undergoing primary KA. Cite this article: Bone Joint Res 2022;11(9):619–628

To examine the minimal detectable change in two patient –based questionnaires for patients with shoulder instability, managed conservatively. Oxford Instability Shoulder Score (OISS) and Shoulder Rating Questionnaire (SRQ) were administered to 93 patients (100 shoulders) attending physiotherapy. Scores were transformed to percentages to allow comparison. Questionnaires were collected at nine months with 5 subjective response categories from “much worse” to “much better”. Score changes were related to subjective response categories and data calculated to ascertain minimal detectable change (MDC) using the method of . McHorney & Tarlov (1995). Proportion of scores over the minimal detectable change score were then examined. 60 patients (64 shoulders) returned questionnaires at nine months. 34 patients (38 shoulders) reported the shoulder was “much better”. The percentage change scores for these patients were significantly different to all other patients (OISS=26%, p< 0.05 and SRQ =20%, p< 0.05). The minimal detectable change score was calculated as 14% for OISS and 10.5% for SRQ. Of the 38 ‘much better’ responses, 32 (i.e. 84%) had a change score > 14% for the OISS and 27 (i.e. 71%) > 10.5% for the SRQ. Of those 7 who responded with ‘no change or worse’, 2/7 (29%) scored > 14% for OISS and 1/7 (14.2%) scored > 10.5%. Minimal detectable change scores have been calculated for the OISS and SRQ in patients with shoulder instability. These may help determine change, which is clinically important in outcome research

Aims. The aim of this study was to perform a cross-cultural adaptation of Oxford Hip Score (OHS) to Indonesian, and to evaluate its psychometric properties. Methods. We performed a cross-cultural adaptation of Oxford Hip Score into Indonesian language (OHS-ID) and determined its internal consistency, test-retest reliability, measurement error, floor-ceiling effect, responsiveness, and construct validity by hypotheses testing of its correlation with Harris Hip Score (HHS), vsual analogue scale (VAS), and Short Form-36 (SF-36). Adults (> 17 years old) with chronic hip pain (osteoarthritis or osteonecrosis) were included. Results. A total of 125 patients were included, including 50 total hip arthroplasty (THA) patients with six months follow-up. The OHS questionnaire was translated into Indonesian and showed good internal consistency (Cronbach’s alpha = 0.89) and good reliability (intraclass correlation = 0.98). The standard error of measurement value of 2.11 resulted in minimal detectable change score of 5.8. Ten out of ten (100%) a priori hypotheses were met, confirming the construct validity. A strong correlation was found with two subscales of SF-36 (pain and physical function), HHS (0.94), and VAS (-0.83). OHS-ID also showed good responsiveness for post-THA series. Floor and ceiling effect was not found. Conclusion. The Indonesian version of OHS showed similar reliability and validity with the original OHS. This questionnaire will be suitable to assess chronic hip pain in Indonesian-speaking patients. Cite this article: Bone Jt Open 2021;2(9):765–772

Introduction. The purpose of this study was to demonstrate the feasibility of passively collecting objective data from a commercially available smartphone-based care management platform (sbCMP) and robotic assisted total knee arthroplasty (raTKA). Methods. Secondary data analysis was performed using de-identified data from a commercial database that collected metrics from a sbCMP combined with intraoperative data collection from raTKA. Patients were included in this analysis if they underwent unilateral raTKA between July 2020 and February 2021, and were prescribed the sbCMP (n=131). The population consisted of 76 females and 55 males, with a mean age of 64 years (range, 43 – 81). Pre-operative through six-week post-operative data included step counts from the sbCMP, as well as administration of the KOOS JR. Intraoperative data included surgical times, the hip-knee-ankle angle (HKA), and medial and lateral laxity assessments from the robotic assessment. Data are presented using descriptive statistics. Comparisons were performed using a paired samples t-test, or Wilcoxon Signed-rank test, with significance assessed at p<0.05. A minimal detectable change (MDC) in the KOOS JR score was considered ½ standard deviation of the preoperative values. Results. KOOS JR scores improved from a preoperative mean of 51.5 ± 11.5 to a 6-week postoperative mean of 64 ± 10.04 (p<0.001). An MDC of 5.75 units was achieved. Step counts decreased initially and returned to preoperative values by week 6 (Figure 1, p=0.196). When evaluating time requirements from landmarking to completed surgical cuts, the median surgical time was 40.2 minutes (IQR, 29.4 – 52.0). The median absolute deformity for HKA preoperatively was 6.9 degrees (IQR, 4.1 – 10.1) and the final intraoperative median HKA was 0.9 degrees (IQR, 0.1 – 3, p<0.001). There was a difference in medial and lateral joint laxity in flexion and extension at the initial intraoperative evaluation (p<0.01). At the final evaluation there was no difference in medial and lateral joint laxity in extension (p=0.239); however, a slight difference in flexion was noted (p=0.001). Given the median values of 1.2mm (0.8 – 2.4) medially vs. 1.4mm (0.9 – 3) laterally, this difference is not likely clinically relevant. Patients who had <1 mm of medial laxity in flexion had significantly fewer step counts at week 6 post-operatively (p=0.035). There was no difference in KOOS JR scores associated with tightness (p>0.05). Discussion. The use of passively collected objective measures in a commercial database across the episode of care was feasible and demonstrated associations between intraoperative and post-operative metrics. To our knowledge, this is the first integrated data collection and reporting platform to report on these measures in a commercial population. Future research is needed in order to understand the benefit of displaying these metrics, as well as the role of variations in alignment and gap balance on function. Conclusions. Contemporary data platforms may be used to improve the understanding of individual recovery paths through real-time passive data collection throughout the episode of care. For any figures or tables, please contact the authors directly

Purpose and background. Static plain radiographs at the end of uncontrolled bending are the current standard of care for measuring translatory slip in back pain patients. Quantitative fluoroscopy systems (QF) that employ standardised bending protocols have been found to improve precision and reduce dose, but comparative data are lacking. We compared 4 QF methods with static radiographs in a control population, calculating ranges, population variation and measurement errors over 6 weeks. Methods. Fifty-four healthy controls (F=22, M=23) received passive recumbent and active weight bearing QF screenings during controlled motion, plus still fluoro imaging in neutral, flexion and extension. The translatory slip of all levels from L2-S1 was determined for each condition using bespoke image tracking codes (Matlab) and pooled to provide means and ranges of variation (+/-1.96SD). The pooled measurement error, or minimal detectable change (MDC. 95. ), reflecting the intra subject repeatability over 6 weeks was calculated. Ranges of translation for each level (L2-S1), for each type of motion were also calculated. Results. Static radiographs at the end of uncontrolled flexion gave the greatest variation and the worst repeatability, while QF recumbent passive and active weight bearing motion with flexion recorded during the motion had ¼ less variation and twice the repeatability. For individual levels, L2-3 had significantly higher flexion ranges in controlled motion than uncontrolled motion, whereas the converse was true at L4-5 (P<0.001). Conclusion. Dynamic QF measurement of flexion translatory slip gives ¼ less population variation and half the measurement error of static radiographs when measured in the same participants. No conflicts of interest. No funding obtained

Background. Dynamic measurement of continuous intervertebral motion in low back pain (LBP) research in-vivo is developing. Lumbar motion parameters with the features of biomarkers are emerging and show promise for advancing understanding of personalised biometrics of LBP. However, measurement of changes over time inevitably involve error, due to subjects' natural variation and/or variation in the measurement process. Thus, intra-subject repeatability of parameters to measure changes over time should be established. Methods. Seven lumbar spine motion parameters, measured using quantitative fluoroscopy (QF), were assessed for intra-subject repeatability: Intervertebral range-of-motion (IV-RoM), laxity, motion sharing inequality (MSI), motion sharing variability (MSV), flexion translation and flexion disc height. Intra-subject reliability (ICC) and minimal detectable change (MDC95) of baseline and 6-week follow-up measurements were obtained for 109 healthy volunteers (54 coronal and 55 sagittal). Results. Reliability was substantial to excellent for repeated measurements of IV-RoM, laxity, flexion translation and disc height during recumbent passive motion (ICC:0.69–0.95) and during active weight-bearing motion (ICC:0.64–0.92). MSI was moderate to excellent across both positions (ICC:0.43–0.91). The reliability of MSV was generally poorer for both positions (0.14–0.65). For all parameters, measurement error exceeded 42%. Conclusion. Recumbent IV-RoM, laxity and disc height demonstrated the best repeatability at 6-weeks suggesting they may be better outcome moderators in clinical studies than other variables. However measurement errors for all parameters were higher than the minimal changes of interest. These results are limited to healthy controls and should be regarded as reference values. Similar studies in CNSLBP patients are required. No conflicts of interest. Sources of Funding: Dr Rebecca Hemming received a Seedcorn Bursary from the Cardiff Institute of Tissue Engineering and Repair (CITER) and Professor Alan Breen received a project grant from the European Chiropractors Union Research Fund (ECURF)

The use of a tourniquet during total knee arthroplasty (TKA) is controversial. Return to function and pain are believed to be affected by the use of a tourniquet. The hypothesis of this study was that use of a tourniquet (T) would delay postoperative functional recovery and increase pain as compared to no tourniquet use (NT). 200 patients were recruited for this prospective, double-blinded, randomized controlled trial. All surgeries were performed by one of two fellowship trained arthroplasty surgeons at our institution. Patients were randomized to either undergo TKA with T or NT and blinded to group allocation. An otherwise standardized perioperative protocol was followed. The primary outcome measures were functional assessment testing using the timed up-and-go (TUG) and stair-climb (SC) tests and visual analog scale pain (VAS-P) scores. Secondary outcome measures included blood loss and range-of-motion (ROM). Patients completed outcomes measures preoperatively, in hospital, and postoperatively at 4–6 weeks and 6–8 months. Minimal detectable change (MDC) and Student's T-test, alpha of p < 0.05, were used to determine significance. No significant differences were seen in postoperative TUG, SC, VAS-P, or ROM at any time point. NT patients were seen to have significantly more calculated blood loss (means: T 1,370.04mL, NT 1,743.85mL; p < 0.001), without a significant increase in transfusion events. Tourniquet use during TKA significantly decreases blood loss and does not adversely affect early postoperative outcomes. Tourniquet use during routine TKA is safe and effective and concerns over deleterious effects on function and pain may not be justified

Objective. Wearable sensors have enabled objective functional data collection from patients before total knee replacement (TKR) and at clinical follow-ups post-surgery whereas traditional evaluation has solely relied on self-reported subjective measures. The timed-up-and-go (TUG) test has been used to evaluate function but is commonly measured using only total completion time, which does not assess joint function or test completion strategy. The current work employs machine learning techniques to distinguish patient groups based on derived functional metrics from the TUG test and expose clinically important functional parameters that are predictive of patient recovery. Methods. Patients scheduled for TKR (n=70) were recruited and instrumented with a wearable sensor system while performing three TUG test trials. Remaining study patients (n=68) also completed three TUG trials at their 2, 6, and 13-week follow-ups. Many patients (n=36) have also participated up to their 26-week appointment. Custom developed software was used to segment recorded tests into sub-activities and extract 54 functional metrics to evaluate op/non-operative knee function. All preoperative TUG samples and their standardized metrics were clustered into two unlabelled groups using the k-means algorithm. Both groups were tracked forward to see how their early functional parameters translated to functional improvement at their three-month assessment. Test total completion time was used to estimate overall functional improvement and to relate findings to existing literature. Patients that completed their 26-week tests were tracked further to their most recent timepoint. Results. Preoperative clustering separated two groups with different test completion times (n=46 vs. n=22 with mean times of 13s vs. 22s). Of the faster preoperative group, 63% of patients maintained their time, 26% improved, and 11% worsened whereas of the slower preoperative group, 27% maintained, 64% improved, and 9% worsened. The high improvement group improved their times by 4.9s (p<0.01) between preoperative and 13-week visits whereas the other group had no significant change. Test times were different between both groups preoperatively (p<0.001) and at 6 (p=0.01) and 13 (p=0.03) weeks but not at 26 weeks (p=0.67). The high improvement group reached an overall improvement of 9s (p<0.01) at 26 weeks whereas the low improvement group still showed no improvement greater than the TUG minimal detectable change of 2.2s (1.8s, p<0.01)[1]. Test sub-activity times for both groups at each timepoint can be seen in Figure 1. Conclusions. This work has demonstrated that machine learning has the potential to find patterns in preoperative functional parameters that can predict functional improvement after surgery. While useful for assigning labels to the distinguished clusters, test completion time was not among the top distinguishable metrics between groups at three months which highlights the necessity for these more descriptive performance metrics when analyzing patient recovery. It is expected that these early predictions will be used to realistically adjust patient expectations or highlight opportunities for physiotherapeutic intervention to improve future outcomes. For any figures or tables, please contact the authors directly

Background and Purpose: A number of authors have calculated thresholds of individually minimally important individual change (MIC) for the Roland Morris Disability Questionnaire (RMDQ). However, at an individual level, the imprecision of the measurement instrument often exceeds the MIC. In recognition of this, there is some consensus on appropriate individual change thresholds (absolute and baseline-specific) for the RMDQ. These were intended to be re-evaluated as further data become available. With this in mind, we calculated the MIC and minimally detectable change (MDC) of the RMDQ in the UK BEAM population. Method and Results: 1,334 patients enrolled in the UK BEAM trial completed the RMDQ. We calculated MIC using ROC curves from three and 12 month follow-up data, and using a seven-point health transition question as the external criterion. We performed sub-analyses of MIC for bands of baseline severity and considered adjusting these for regression to the mean (RTM). We calculated MDC based on within-person and residual error variances of stable patients’ repeated measurements. The overall MIC was four points and the MDC 7.6 points. These values fall around the centre of the ranges considered by the consensus study team. Higher MIC values were observed for more disabled patients; this may be partially an artefact of RTM. In our positively skewed population, more disabled patients required more than the consensus recommendation of 30% change from baseline. Conclusion: This is further evidence that five RMDQ points is an appropriate threshold by which to judge individual change on the RMDQ. Proportional change from baseline may be more population-specific than previously thought

Aims

A substantial fraction of patients undergoing knee arthroplasty (KA) or hip arthroplasty (HA) do not achieve an improvement as high as the minimal clinically important difference (MCID), i.e. do not achieve a meaningful improvement. Using three patient-reported outcome measures (PROMs), our aim was: 1) to assess machine learning (ML), the simple pre-surgery PROM score, and logistic-regression (LR)-derived performance in their prediction of whether patients undergoing HA or KA achieve an improvement as high or higher than a calculated MCID; and 2) to test whether ML is able to outperform LR or pre-surgery PROM scores in predictive performance.

The peak external knee adduction moment during walking gait has been proposed to be a clinically useful measure of dynamic knee joint load in patients with knee osteoarthritis. However, there is limited information about the reliability of this measure, or its ability to detect change. The test-retest reliability and sensitivity to change of peak knee adduction moments were evaluated in thirty patients with varus gonarthrosis. Indices of relative and absolute reliability were excellent (intra-class correlation coefficient = 0.85, standard error of measurement = 0.36 % BW*Ht), and the sensitivity to change following high tibial osteotomy was high (standardized response mean = 1.2). To estimate the test-retest reliability, measurement error and sensitivity to change of the peak knee adduction moment during gait. Thirty patients (44”11 yrs, 1.7”0.09 m, 87”20 kg, twenty males, ten females) with varus gonarthrosis underwent gait analyses on two pre-operative test occasions within one week, and on a third test occasion six months after medial opening wedge high tibial osteotomy. Three-dimensional kinematic and kinetic gait data were collected during self-paced walking and used to calculate the peak knee adduction moment. An intraclass correlation coefficient of 0.85 (95%CI: 0.71, 0.93) indicated excellent relative reliability, and a standard error of measurement of 0.36 %BW*Ht (95%CI: 0.29, 0.49) indicated low measurement error. The peak knee adduction moment after surgery (1.66”0.72 %BW*Ht) was significantly (p< 0.001) lower than before surgery (2.58”0.72 %BW*Ht). A standardized response mean of 1.2 (95%CI: 0.77, 1.6) indicated the size of this change was large. Based on 95% confidence levels, these results suggest the error in an individual’s peak knee adduction moment at one point in time is 0.70 % BW*Ht, the minimal detectable change in an individual’s peak adduction moment is 1.0 %BW*Ht, and it is sensitive to change following treatment. The peak knee adduction moment during gait has appropriate reliability for use in studies evaluating the effect of treatments intended to decrease the load on the knee. When considering measurement error, the knee adduction moment is also appropriate for clinical use in evaluating change in individual patients. Funding: CIHR, Arthrex Inc

Aims

The Single Assessment Numerical Evalution (SANE) score is a pragmatic alternative to longer patient-reported outcome measures (PROMs). The purpose of this study was to investigate the concurrent validity of the SANE and hip-specific PROMs in a generalized population of patients with hip pain at a single timepoint upon initial visit with an orthopaedic surgeon who is a hip preservation specialist. We hypothesized that SANE would have a strong correlation with the 12-question International Hip Outcome Tool (iHOT)-12, the Hip Outcome Score (HOS), and the Hip disability and Osteoarthritis Outcome Score (HOOS), providing evidence for concurrent validity of the SANE and hip-specific outcome measures in patients with hip pain.

Aims

Treatment of Weber B ankle fractures that are stable on weightbearing radiographs but unstable on concomitant stress tests (classified SER4a) is controversial. Recent studies indicate that these fractures should be treated nonoperatively, but no studies have compared alternative nonoperative options. This study aims to evaluate patient-reported outcomes and the safety of fracture treatment using functional orthosis versus cast immobilization.

Aims

The primary aim of this study was to present the mid-term follow-up of a multicentre randomized controlled trial (RCT) which compared the functional outcome following routine removal (RR) to the outcome following on-demand removal (ODR) of the syndesmotic screw (SS).

Aims

This study aimed to investigate the relationship between changes in patellar height and clinical outcomes at a mean follow-up of 7.7 years (5 to 10) after fixed-bearing posterior-stabilized total knee arthroplasty (PS-TKA).

Aims

Avulsion of the proximal hamstring tendon origin can result in significant functional impairment, with surgical re-attachment of the tendons becoming an increasingly recognized treatment. The aim of this study was to assess the outcomes of surgical management of proximal hamstring tendon avulsions, and to compare the results between acute and chronic repairs, as well as between partial and complete injuries.

The December 2015 Shoulder & Elbow Roundup360 looks at:

Objectives

The aim of this study was to systematically review the literature on measurement of muscle strength in patients with femoroacetabular impingement (FAI) and other pathologies and to suggest guidelines to standardise protocols for future research in the field.

The August 2012 Shoulder & Elbow Roundup³⁶⁰ looks at: platelet-rich fibrin matrix and the torn rotator cuff; ultrasound, trainees, and ducks out of water; the torn rotator cuff and conservative treatment; Bankart repair and subsequent degenerative change; proprioception after shoulder replacement; surgery for a terrible triad, with reasonable short-term results; and the WORC Index.